-
1
-
-
0000244405
-
Über die beziehungen der senilen hirnatrophie zur aphasie
-
Pick A (1892) Über die Beziehungen der senilen Hirnatrophie zur Aphasie. Prager Med Wochenschr 16:765-767
-
(1892)
Prager Med Wochenschr
, vol.16
, pp. 765-767
-
-
Pick, A.1
-
2
-
-
33646906138
-
Über eigenartige krankheitsfälle des späteren alters
-
Alzheimer A (1911) Über eigenartige Krankheitsfälle des späteren Alters. Z ges Neurol Psychiat 4:356-385
-
(1911)
Z Ges Neurol Psychiat
, vol.4
, pp. 356-385
-
-
Alzheimer, A.1
-
3
-
-
0014370449
-
Electron microscopic structure of the inclusion bodies in Pick's disease
-
Rewcastle NB, Ball MJ (1968) Electron microscopic structure of the inclusion bodies in Pick's disease. Neurology 18:1205-1213
-
(1968)
Neurology
, vol.18
, pp. 1205-1213
-
-
Rewcastle, N.B.1
Ball, M.J.2
-
4
-
-
0022976136
-
Filamentous aggregates in Pick's disease, progressive supranuclear palsy, and Alzheimer's disease share antigenic determinants with microtubule-associated protein tau
-
Pollock NJ, Mirra SS, Binder LI, Hansen LA, Wood JG (1986) Filamentous aggregates in Pick's disease, progressive supranuclear palsy, and Alzheimer's disease share antigenic determinants with microtubule-associated protein tau. Lancet II:1211
-
(1986)
Lancet
, vol.2
, pp. 1211
-
-
Pollock, N.J.1
Mirra, S.S.2
Binder, L.I.3
Hansen, L.A.4
Wood, J.G.5
-
5
-
-
0029850476
-
Pick's disease: Hyperphosphorylated tau segregates to the somatoaxonal compartment
-
Probst A, Tolnay M, Langui D, Goedert M, Spillantini MG (1996) Pick's disease: hyperphosphorylated tau segregates to the somatoaxonal compartment. Acta Neuropathol (Berl) 92:588-596
-
(1996)
Acta Neuropathol (Berl)
, vol.92
, pp. 588-596
-
-
Probst, A.1
Tolnay, M.2
Langui, D.3
Goedert, M.4
Spillantini, M.G.5
-
6
-
-
0000293742
-
Über eine eigenartige erkrankung der hirnrinde
-
Alzheimer A (1907) Über eine eigenartige Erkrankung der Hirnrinde. Allg Z Psychiat Psych Gerichtl Med 64:146-148
-
(1907)
Allg Z Psychiat Psych Gerichtl Med
, vol.64
, pp. 146-148
-
-
Alzheimer, A.1
-
7
-
-
0003374626
-
Tau protein pathology in neurodegenerative diseases
-
Spillantini MG, Goedert M (1998) Tau protein pathology in neurodegenerative diseases. Trends Neurosci 21:428-433
-
(1998)
Trends Neurosci
, vol.21
, pp. 428-433
-
-
Spillantini, M.G.1
Goedert, M.2
-
8
-
-
0028073692
-
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
-
Wilhelmsen KC, Lynch T, Pavlou E, Higgins M, Nygaard TG (1994) Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. Am J Hum Genet 55:1159-1165
-
(1994)
Am J Hum Genet
, vol.55
, pp. 1159-1165
-
-
Wilhelmsen, K.C.1
Lynch, T.2
Pavlou, E.3
Higgins, M.4
Nygaard, T.G.5
-
9
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus statement
-
Foster NL, Wilhelmsen KC, Sima AAF, Jones MZ, D'Amato C, Oilman S, Spillantini MG, Lynch T, Mayeux RP, Gaskell PC, Hulette C, Pericak-Vance MA, Welsh-Bohmer KA, Dickson DW, Heutink P, Kros J, Van Swieten JC, Arwert F, Ghetti B, Murrell J, Lannfelt L, Hutton M, Phelps CH, Snyder DS, Oliver E, Ball MJ, Cummings JL, Miller BL, Katzman R, Reed L, Schelper RL, Lanska DJ, Brun A, Fink JK, Khul DE, Knopman DS, Wszolek Z, Miller CL, Bird TD, Lendon C, Elechi C (1997) Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus statement. Ann Neurol 41:706-715
-
(1997)
Ann Neurol
, vol.41
, pp. 706-715
-
-
Foster, N.L.1
Wilhelmsen, K.C.2
Sima, A.A.F.3
Jones, M.Z.4
D'Amato, C.5
Oilman, S.6
Spillantini, M.G.7
Lynch, T.8
Mayeux, R.P.9
Gaskell, P.C.10
Hulette, C.11
Pericak-Vance, M.A.12
Welsh-Bohmer, K.A.13
Dickson, D.W.14
Heutink, P.15
Kros, J.16
Van Swieten, J.C.17
Arwert, F.18
Ghetti, B.19
Murrell, J.20
Lannfelt, L.21
Hutton, M.22
Phelps, C.H.23
Snyder, D.S.24
Oliver, E.25
Ball, M.J.26
Cummings, J.L.27
Miller, B.L.28
Katzman, R.29
Reed, L.30
Schelper, R.L.31
Lanska, D.J.32
Brun, A.33
Fink, J.K.34
Khul, D.E.35
Knopman, D.S.36
Wszolek, Z.37
Miller, C.L.38
Bird, T.D.39
Lendon, C.40
Elechi, C.41
more..
-
10
-
-
0031949084
-
Frontotemporal dementia and parkinsonism linked to chromosome 17:A new group of tauopathies
-
Spillantini MG, Bird TD, Ghetti B (1998) Frontotemporal dementia and parkinsonism linked to chromosome 17:a new group of tauopathies. Brain Pathol 8:387-402
-
(1998)
Brain Pathol
, vol.8
, pp. 387-402
-
-
Spillantini, M.G.1
Bird, T.D.2
Ghetti, B.3
-
11
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, Andreadis A, Wiederholt WC, Raskind M, Schellenberg GD (1998) Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol 43:815-825
-
(1998)
Ann Neurol
, vol.43
, pp. 815-825
-
-
Poorkaj, P.1
Bird, T.D.2
Wijsman, E.3
Nemens, E.4
Garruto, R.M.5
Anderson, L.6
Andreadis, A.7
Wiederholt, W.C.8
Raskind, M.9
Schellenberg, G.D.10
-
12
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, Graaff E de, Wauters E, Van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JBJ, Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, Van Swieten J, Mann D, Lynch T, Heutink P (1998) Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 393:702-705
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.6
Pickering-Brown, S.7
Chakraverty, S.8
Isaacs, A.9
Grover, A.10
Hackett, J.11
Adamson, J.12
Lincoln, S.13
Dickson, D.14
Davies, P.15
Petersen, R.C.16
Stevens, M.17
De Graaff, E.18
Wauters, E.19
Van Baren, J.20
Hillebrand, M.21
Joosse, M.22
Kwon, J.M.23
Nowotny, P.24
Che, L.K.25
Norton, J.26
Morris, J.C.27
Reed, L.A.28
Trojanowski, J.29
Basun, H.30
Lannfelt, L.31
Neystat, M.32
Fahn, S.33
Dark, F.34
Tannenberg, T.35
Dodd, P.R.36
Hayward, N.37
Kwok, J.B.J.38
Schofield, P.R.39
Andreadis, A.40
Snowden, J.41
Craufurd, D.42
Neary, D.43
Owen, F.44
Oostra, B.A.45
Hardy, J.46
Goate, A.47
Van Swieten, J.48
Mann, D.49
Lynch, T.50
Heutink, P.51
more..
-
13
-
-
0032560487
-
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
-
Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B (1998) Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc Natl Acad Sci U S A 95:7737-7741
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 7737-7741
-
-
Spillantini, M.G.1
Murrell, J.R.2
Goedert, M.3
Farlow, M.R.4
Klug, A.5
Ghetti, B.6
-
14
-
-
0002792366
-
Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease
-
Goedert M, Wischik CM, Crowther RA, Walker JE, Klug A (1988) Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease. Proc Natl Acad Sci U S A 85:4051-4055
-
(1988)
Proc Natl Acad Sci U S A
, vol.85
, pp. 4051-4055
-
-
Goedert, M.1
Wischik, C.M.2
Crowther, R.A.3
Walker, J.E.4
Klug, A.5
-
15
-
-
0024387161
-
Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats; differential expression of tau protein mRNAs in human brain
-
Goedert M, Spillantini MG, Potier MC, Ulrich J, Crowther RA (1989) Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats; differential expression of tau protein mRNAs in human brain. EMBO J 8:393-399
-
(1989)
EMBO J
, vol.8
, pp. 393-399
-
-
Goedert, M.1
Spillantini, M.G.2
Potier, M.C.3
Ulrich, J.4
Crowther, R.A.5
-
16
-
-
0024745894
-
Multiple isoforms of human microtubule-associated protein tau: Sequences and localization in neurofibrillary tangles of Alzheimer's disease
-
Goedert M, Spillantini MG, Jakes R, Rutherford D, Crowther RA (1989) Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease. Neuron 3:519-526
-
(1989)
Neuron
, vol.3
, pp. 519-526
-
-
Goedert, M.1
Spillantini, M.G.2
Jakes, R.3
Rutherford, D.4
Crowther, R.A.5
-
17
-
-
0025600995
-
Expression of separate isoforms of human tau protein: Correlation with the tau pattern in brain and effects on tubulin polymerization
-
Goedert M, Jakes R (1990) Expression of separate isoforms of human tau protein: correlation with the tau pattern in brain and effects on tubulin polymerization. EMBO J 9:4225-4230
-
(1990)
EMBO J
, vol.9
, pp. 4225-4230
-
-
Goedert, M.1
Jakes, R.2
-
18
-
-
0026488111
-
Structure and novel exons of the human tau gene
-
Andreadis A, Brown MW, Kosik KS (1992) Structure and novel exons of the human tau gene. Biochemistry 31:10626-10633
-
(1992)
Biochemistry
, vol.31
, pp. 10626-10633
-
-
Andreadis, A.1
Brown, M.W.2
Kosik, K.S.3
-
19
-
-
0028027088
-
Domains of tau protein and interaction with microlubules
-
Gustke N, Trinczek B, Biernat J, Mandelkow EM, Mandelkow E (1994) Domains of tau protein and interaction with microlubules. Biochemistry 33:9511-9522
-
(1994)
Biochemistry
, vol.33
, pp. 9511-9522
-
-
Gustke, N.1
Trinczek, B.2
Biernat, J.3
Mandelkow, E.M.4
Mandelkow, E.5
-
20
-
-
0028175215
-
Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau
-
Goode BL, Feinstein SC (1994) Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau. J Cell Biol 124:769-782
-
(1994)
J Cell Biol
, vol.124
, pp. 769-782
-
-
Goode, B.L.1
Feinstein, S.C.2
-
21
-
-
7344220963
-
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism
-
Dumanchin C, Camuzat A, Campion D, Verpillat P, Hannequin D, Dubois B, Saugier-Veber P, Martin C, Penet C, Charbonnier F, Agid Y, Frebourg T, Brice A (1998) Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism. Hum Mol Genet 7:1825-1829
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1825-1829
-
-
Dumanchin, C.1
Camuzat, A.2
Campion, D.3
Verpillat, P.4
Hannequin, D.5
Dubois, B.6
Saugier-Veber, P.7
Martin, C.8
Penet, C.9
Charbonnier, F.10
Agid, Y.11
Frebourg, T.12
Brice, A.13
-
22
-
-
0032573083
-
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
-
Clark LN, Poorkaj P, Wszolek Z, Geschwind DH, Nasreddine ZS, Miller B, Li D, Payami H, Awert F, Markopoulou K, Andreadis A, D'Souza I, Lee VM-Y, Reed L, Trojanowski JQ, Zhukareva V, Bird T, Schellenberg G, Wilhelmsen KC (1998) Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. Proc Natl Acad Sci U S A 95:13103-13107
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 13103-13107
-
-
Clark, L.N.1
Poorkaj, P.2
Wszolek, Z.3
Geschwind, D.H.4
Nasreddine, Z.S.5
Miller, B.6
Li, D.7
Payami, H.8
Awert, F.9
Markopoulou, K.10
Andreadis, A.11
D'Souza, I.12
Lee, V.-Y.13
Reed, L.14
Trojanowski, J.Q.15
Zhukareva, V.16
Bird, T.17
Schellenberg, G.18
Wilhelmsen, K.C.19
-
23
-
-
0033070197
-
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands
-
Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, Van Duijn CM, Heutink P (1999) High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. Am J Hum Genet 64:414-421
-
(1999)
Am J Hum Genet
, vol.64
, pp. 414-421
-
-
Rizzu, P.1
Van Swieten, J.C.2
Joosse, M.3
Hasegawa, M.4
Stevens, M.5
Tibben, A.6
Niermeijer, M.F.7
Hillebrand, M.8
Ravid, R.9
Oostra, B.A.10
Goedert, M.11
Van Duijn, C.M.12
Heutink, P.13
-
24
-
-
0033602013
-
A distinct familial presenile dementia with a novel missense mutation in the tau gene
-
Iijima M, Tabira T, Poorkaj P, Schellenberg GD, Trojanowski JQ, Lee VM-Y, Schmidt ML, Takahashi K, Nabika T, Matsumoto T, Yamashita Y, Yoshioka S, Ishino H (1999) A distinct familial presenile dementia with a novel missense mutation in the tau gene. Neuroreport 10:497-501
-
(1999)
Neuroreport
, vol.10
, pp. 497-501
-
-
Iijima, M.1
Tabira, T.2
Poorkaj, P.3
Schellenberg, G.D.4
Trojanowski, J.Q.5
Lee, V.-Y.6
Schmidt, M.L.7
Takahashi, K.8
Nabika, T.9
Matsumoto, T.10
Yamashita, Y.11
Yoshioka, S.12
Ishino, H.13
-
25
-
-
0032965787
-
Mutations in the tau exon 10 splice site region in familial frontotemporal dementia
-
Morris HR, Perez-Tur J, Janssen JC, Brown J, Lees AJ, Wood NW, Hardy J, Hutton M, Rossor MN (1999) Mutations in the tau exon 10 splice site region in familial frontotemporal dementia. Ann Neurol 45:270-271
-
(1999)
Ann Neurol
, vol.45
, pp. 270-271
-
-
Morris, H.R.1
Perez-Tur, J.2
Janssen, J.C.3
Brown, J.4
Lees, A.J.5
Wood, N.W.6
Hardy, J.7
Hutton, M.8
Rossor, M.N.9
-
26
-
-
0032950744
-
Tau gene mutation in familial progressive subcortical gliosis
-
Goedert M, Spillantini MG, Crowther RA, Chen SG, Parchi P, Tabaton M, Lanska DJ, Markesbery WR, Wilhelmsen KC, Dickson DW, Petersen RB, Gambetti P (1999) Tau gene mutation in familial progressive subcortical gliosis. Nat Med 5:454-457
-
(1999)
Nat Med
, vol.5
, pp. 454-457
-
-
Goedert, M.1
Spillantini, M.G.2
Crowther, R.A.3
Chen, S.G.4
Parchi, P.5
Tabaton, M.6
Lanska, D.J.7
Markesbery, W.R.8
Wilhelmsen, K.C.9
Dickson, D.W.10
Petersen, R.B.11
Gambetti, P.12
-
27
-
-
0032920233
-
Tau pathology in a family with dementia and a P301L mutation in tau
-
Mirra SS, Murrell JR, Gearing M, Spillantini MG, Goedert M, Crowther RA, Levey AI, Jones R, Green J, Shoffner JM, Wainer BH, Schmidt ML, Trojanowski JQ, Ghetti B (1999) Tau pathology in a family with dementia and a P301L mutation in tau. J Neuropathol Exp Neurol 58:335-345
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 335-345
-
-
Mirra, S.S.1
Murrell, J.R.2
Gearing, M.3
Spillantini, M.G.4
Goedert, M.5
Crowther, R.A.6
Levey, A.I.7
Jones, R.8
Green, J.9
Shoffner, J.M.10
Wainer, B.H.11
Schmidt, M.L.12
Trojanowski, J.Q.13
Ghetti, B.14
-
28
-
-
0032897924
-
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
-
Bird TD, Nochljn D, Poorkaj P, Cherrier M, Kaye J, Payami H, Peskind E, Lampe TH, Nemens E, Boyer PJ, Schellenberg GD (1999) A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L). Brain 122:741-756
-
(1999)
Brain
, vol.122
, pp. 741-756
-
-
Bird, T.D.1
Nochljn, D.2
Poorkaj, P.3
Cherrier, M.4
Kaye, J.5
Payami, H.6
Peskind, E.7
Lampe, T.H.8
Nemens, E.9
Boyer, P.J.10
Schellenberg, G.D.11
-
29
-
-
0033545946
-
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17, by affecting multiple alternative RNA splicing regulatory elements
-
D'Souza I, Poorkaj P, Hong M, Nochlin D, Lee VM-Y, Bird T, Schellenberg GD (1999) Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17, by affecting multiple alternative RNA splicing regulatory elements. Proc Natl Acad Sci USA 96:5598-5603
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 5598-5603
-
-
D'Souza, I.1
Poorkaj, P.2
Hong, M.3
Nochlin, D.4
Lee, V.-Y.5
Bird, T.6
Schellenberg, G.D.7
-
30
-
-
0033059975
-
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in Tau
-
Bugiani O, Murrell JR, Giaccone G, Hasegawa M, Ghigo G, Tabaton M, Morbin M, Primavera A, Carella F, Solaro C, Grisoli M, Savoiardo M, Spillantini MG, Tagliavini F, Goedert M, Ghetti B (1999) Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in Tau. J Neuropathol Exp Neurol 58:667-677
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 667-677
-
-
Bugiani, O.1
Murrell, J.R.2
Giaccone, G.3
Hasegawa, M.4
Ghigo, G.5
Tabaton, M.6
Morbin, M.7
Primavera, A.8
Carella, F.9
Solaro, C.10
Grisoli, M.11
Savoiardo, M.12
Spillantini, M.G.13
Tagliavini, F.14
Goedert, M.15
Ghetti, B.16
-
31
-
-
0032976201
-
From genotype to phenotype: A clinical, pathological and biochemical investigation of fronto-temporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation
-
Nasreddine ZS, Loginov M, Clark LN, Lamarche J, Miller BL, Lamontagne A, Zhukareva V, Lee VM-Y, Wilhelmsen KC, Geschwind DH (1999) From genotype to phenotype: a clinical, pathological and biochemical investigation of fronto-temporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation. Ann Neurol 45:704-715
-
(1999)
Ann Neurol
, vol.45
, pp. 704-715
-
-
Nasreddine, Z.S.1
Loginov, M.2
Clark, L.N.3
Lamarche, J.4
Miller, B.L.5
Lamontagne, A.6
Zhukareva, V.7
Lee, V.-Y.8
Wilhelmsen, K.C.9
Geschwind, D.H.10
-
32
-
-
0033002879
-
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy
-
Delisle MB, Murrell JR, Richardson R, Trofatter JA, Rascol O, Soulages X, Mohr M, Calvas P, Ghetti B (1999) A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy. Acta Neuropathol (Berl) 98:62-77
-
(1999)
Acta Neuropathol (Berl)
, vol.98
, pp. 62-77
-
-
Delisle, M.B.1
Murrell, J.R.2
Richardson, R.3
Trofatter, J.A.4
Rascol, O.5
Soulages, X.6
Mohr, M.7
Calvas, P.8
Ghetti, B.9
-
33
-
-
0032837303
-
Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia
-
Houlden H, Baker M, Adamson J, Grover A, Waring S, Dickson D, Lynch T, Boeve B, Petersen RC, Pickering-Brown S, Owen F, Neary D, Craufurd D, Snowden J, Mann D, Hutton M (1999) Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia. Ann Neurol 46:243-248
-
(1999)
Ann Neurol
, vol.46
, pp. 243-248
-
-
Houlden, H.1
Baker, M.2
Adamson, J.3
Grover, A.4
Waring, S.5
Dickson, D.6
Lynch, T.7
Boeve, B.8
Petersen, R.C.9
Pickering-Brown, S.10
Owen, F.11
Neary, D.12
Craufurd, D.13
Snowden, J.14
Mann, D.15
Hutton, M.16
-
34
-
-
0032815068
-
Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke family 1684
-
Hulette CM, Pericak-Vance MA, Roses AD, Schmechel DE, Yamaoka LH, Gaskell PC, Welsh-Bohmer KA, Crowther RA, Spillantini MG (1999) Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke family 1684. J Neuropathol Exp Neurol 58:859-866
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 859-866
-
-
Hulette, C.M.1
Pericak-Vance, M.A.2
Roses, A.D.3
Schmechel, D.E.4
Yamaoka, L.H.5
Gaskell, P.C.6
Welsh-Bohmer, K.A.7
Crowther, R.A.8
Spillantini, M.G.9
-
35
-
-
0033546987
-
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration
-
Yasuda M, Kawamata T, Komure O, Kuno S, D'Souza I, Poorkaj P, Kawai J, Tanimukai S, Yamamoto Y, Hasegawa H, Sasahara M, Hazama F, Schellenberg GD, Tanaka C (1999) A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration. Neurology 53:864-868
-
(1999)
Neurology
, vol.53
, pp. 864-868
-
-
Yasuda, M.1
Kawamata, T.2
Komure, O.3
Kuno, S.4
D'Souza, I.5
Poorkaj, P.6
Kawai, J.7
Tanimukai, S.8
Yamamoto, Y.9
Hasegawa, H.10
Sasahara, M.11
Hazama, F.12
Schellenberg, G.D.13
Tanaka, C.14
-
36
-
-
0032880430
-
Phenotypic variation in hereditary frontotemporal dementia with tau mutations
-
Van Swieten JC, Stevens M, Rosso SM, Rizzu P, Joosse M, Koning I de, Kamphorst W, Ravid R, Spillantini MG, Niermeijer MF, Heutink P (1999) Phenotypic variation in hereditary frontotemporal dementia with tau mutations. Ann Neurol 46:617-626
-
(1999)
Ann Neurol
, vol.46
, pp. 617-626
-
-
Van Swieten, J.C.1
Stevens, M.2
Rosso, S.M.3
Rizzu, P.4
Joosse, M.5
De Koning, I.6
Kamphorst, W.7
Ravid, R.8
Spillantini, M.G.9
Niermeijer, M.F.10
Heutink, P.11
-
37
-
-
0032763203
-
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits
-
Murrell JR, Spillantini MG, Zolo P, Guazzelli M, Smith MJ, Hasegawa M, Redi F, Crowther RA, Pietrini P, Ghetti B, Goedert M (1999) Tau gene mutation G389R causes a tauopathy with abundant Pick body-like inclusions and axonal deposits. J Neuropathol Exp Neurol 58:1207-1226
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 1207-1226
-
-
Murrell, J.R.1
Spillantini, M.G.2
Zolo, P.3
Guazzelli, M.4
Smith, M.J.5
Hasegawa, M.6
Redi, F.7
Crowther, R.A.8
Pietrini, P.9
Ghetti, B.10
Goedert, M.11
-
38
-
-
0032561415
-
Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly
-
Hasegawa M, Smith MJ, Goedert M (1998) Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly. FEBS Lett 437:207-210
-
(1998)
FEBS Lett
, vol.437
, pp. 207-210
-
-
Hasegawa, M.1
Smith, M.J.2
Goedert, M.3
-
39
-
-
0032484089
-
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17
-
Hong M, Zhukareva V, Vogelsberg-Ragaglia V, Wszolek Z, Reed L, Miller BL, Geschwind DH, Bird TD, McKeel D, Goate A, Morris JC, Wilhelmsen KC, Schellenberg GD, Trojanowski JQ, Lee VM-Y (1998) Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. Science 282:1914-1917
-
(1998)
Science
, vol.282
, pp. 1914-1917
-
-
Hong, M.1
Zhukareva, V.2
Vogelsberg-Ragaglia, V.3
Wszolek, Z.4
Reed, L.5
Miller, B.L.6
Geschwind, D.H.7
Bird, T.D.8
McKeel, D.9
Goate, A.10
Morris, J.C.11
Wilhelmsen, K.C.12
Schellenberg, G.D.13
Trojanowski, J.Q.14
Lee, V.-Y.15
-
40
-
-
0033042978
-
Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation
-
Dayanandan R, Van Slegtenhorst M, Mack TGA, Ko L, Yen S-H, Leroy K, Brion JP, Anderton BH, Hutton M, Lovestone S (1999) Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation. FEBS Lett 446:228-232
-
(1999)
FEBS Lett
, vol.446
, pp. 228-232
-
-
Dayanandan, R.1
Van Slegtenhorst, M.2
Mack, T.G.A.3
Ko, L.4
Yen, S.-H.5
Leroy, K.6
Brion, J.P.7
Anderton, B.H.8
Hutton, M.9
Lovestone, S.10
-
41
-
-
0033011181
-
Accelerated filament formation from tau protein with specific FTDP-17 missense mutations
-
Nacharaju P, Lewis J, Easson C, Yen S, Hackett J, Hutton M, Yen S-H (1999) Accelerated filament formation from tau protein with specific FTDP-17 missense mutations. FEBS Lett 447:195-199
-
(1999)
FEBS Lett
, vol.447
, pp. 195-199
-
-
Nacharaju, P.1
Lewis, J.2
Easson, C.3
Yen, S.4
Hackett, J.5
Hutton, M.6
Yen, S.-H.7
-
42
-
-
0032919462
-
Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments
-
Goedert M, Jakes R, Crowther RA (1999) Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments. FEBS Lett 450:306-311
-
(1999)
FEBS Lett
, vol.450
, pp. 306-311
-
-
Goedert, M.1
Jakes, R.2
Crowther, R.A.3
-
43
-
-
0345561533
-
Polymerization of tau peptides into fibrillar structures. The effect of FTDP-17 mutations
-
Arrasate M, Pérez M, Armas-Portela, Avila J (1999) Polymerization of tau peptides into fibrillar structures. The effect of FTDP-17 mutations. FEBS Lett 446:199-202
-
(1999)
FEBS Lett
, vol.446
, pp. 199-202
-
-
Arrasate, M.1
Pérez, M.2
Armas-Portela3
Avila, J.4
-
44
-
-
0033529304
-
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17
-
Varani L, Hasegawa M, Spillantini MG, Smith MJ, Murrell JR, Ghetti B, Klug A, Goedert M, Varani G (1999) Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17. Proc Natl Acad Sci U S A 96:8229-8234
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 8229-8234
-
-
Varani, L.1
Hasegawa, M.2
Spillantini, M.G.3
Smith, M.J.4
Murrell, J.R.5
Ghetti, B.6
Klug, A.7
Goedert, M.8
Varani, G.9
-
45
-
-
0033591225
-
5′ Splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10
-
Grover A, Houlden H, Baker M, Adamson J, Lewis J, Prihar G, Pickering-Brown S, Duff K, Hutton, M (1999) 5′ Splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10. J Biol Chem 274:15134-15143
-
(1999)
J Biol Chem
, vol.274
, pp. 15134-15143
-
-
Grover, A.1
Houlden, H.2
Baker, M.3
Adamson, J.4
Lewis, J.5
Prihar, G.6
Pickering-Brown, S.7
Duff, K.8
Hutton, M.9
-
46
-
-
0033060662
-
FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10
-
Hasegawa M, Smith MJ, Iijima M, Tabira T, Goedert M (1999) FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10. FEBS Lett 443:93-96
-
(1999)
FEBS Lett
, vol.443
, pp. 93-96
-
-
Hasegawa, M.1
Smith, M.J.2
Iijima, M.3
Tabira, T.4
Goedert, M.5
-
47
-
-
0026567475
-
Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala
-
Sumi SM, Bird TD, Nochlin D, Raskind MA (1992) Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala. Neurology 42:120-127
-
(1992)
Neurology
, vol.42
, pp. 120-127
-
-
Sumi, S.M.1
Bird, T.D.2
Nochlin, D.3
Raskind, M.A.4
-
48
-
-
0026775551
-
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration
-
Wszolek ZK, Pfeiffer RF, Bhatt MH, Schelper RL, Cordes M, Snow BJ, Rodnitzky RL, Wolters E, Sarwert F, Calne DB (1992) Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration. Ann Neurol 32:312-320
-
(1992)
Ann Neurol
, vol.32
, pp. 312-320
-
-
Wszolek, Z.K.1
Pfeiffer, R.F.2
Bhatt, M.H.3
Schelper, R.L.4
Cordes, M.5
Snow, B.J.6
Rodnitzky, R.L.7
Wolters, E.8
Sarwert, F.9
Calne, D.B.10
-
49
-
-
0027948959
-
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex
-
Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AAF, Keohane C, Nygaard TG, Fahn S, Mayeux R, Rowland LP, Wilhelmsen KC (1994) Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. Neurology 44:1878-1884
-
(1994)
Neurology
, vol.44
, pp. 1878-1884
-
-
Lynch, T.1
Sano, M.2
Marder, K.S.3
Bell, K.L.4
Foster, N.L.5
Defendini, R.F.6
Sima, A.A.F.7
Keohane, C.8
Nygaard, T.G.9
Fahn, S.10
Mayeux, R.11
Rowland, L.P.12
Wilhelmsen, K.C.13
-
50
-
-
0028040918
-
Familial progressive subcortical gliosis
-
Lanska DJ, Currier RD, Cohen M, Gambetti P, Smith EE, Bebin J, Jackson JF, Whitehouse PJ, Markesbery WR (1994) Familial progressive subcortical gliosis. Neurology 44:1633-1643
-
(1994)
Neurology
, vol.44
, pp. 1633-1643
-
-
Lanska, D.J.1
Currier, R.D.2
Cohen, M.3
Gambetti, P.4
Smith, E.E.5
Bebin, J.6
Jackson, J.F.7
Whitehouse, P.J.8
Markesbery, W.R.9
-
51
-
-
0029064004
-
Familial progressive subcortical gliosis. Presence of prions and linkage to chromosome 17
-
Petersen RB, Tabaton M, Chen SG, Monari L, Richardson SL, Lynch T, Manetto V, Lanska DJ, Markesbery WR, Currier RD, Autilio-Gambetti L, Wilhelmsen KC, Gambetti P (1995) Familial progressive subcortical gliosis. Presence of prions and linkage to chromosome 17. Neurology 45:1062-1067
-
(1995)
Neurology
, vol.45
, pp. 1062-1067
-
-
Petersen, R.B.1
Tabaton, M.2
Chen, S.G.3
Monari, L.4
Richardson, S.L.5
Lynch, T.6
Manetto, V.7
Lanska, D.J.8
Markesbery, W.R.9
Currier, R.D.10
Autilio-Gambetti, L.11
Wilhelmsen, K.C.12
Gambetti, P.13
-
52
-
-
0031045491
-
Hereditary fronto-temporal dementia is linked to chromosome 17q21-22. A genetic and clinico-pathological study of three Dutch families
-
Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, Van Duijn CM, Oostra BA, Van Swieten JC (1997) Hereditary fronto-temporal dementia is linked to chromosome 17q21-22. A genetic and clinico-pathological study of three Dutch families. Ann Neurol 41:150-159
-
(1997)
Ann Neurol
, vol.41
, pp. 150-159
-
-
Heutink, P.1
Stevens, M.2
Rizzu, P.3
Bakker, E.4
Kros, J.M.5
Tibben, A.6
Niermeijer, M.F.7
Van Duijn, C.M.8
Oostra, B.A.9
Van Swieten, J.C.10
-
53
-
-
15444356436
-
Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22
-
Baker M, Kwok J, Kucera S, Crook R, Farrer M, Houlden H, Isaacs A, Lincoln S, Onstead L, Hardy J, Wittenberg L, Dodd P, Webb S, Hayward N, Tannenberg T, Andreadis A, Hallupp M, Schofield P, Dark F, Hutton M (1997) Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22. Ann Neurol 42:794-798
-
(1997)
Ann Neurol
, vol.42
, pp. 794-798
-
-
Baker, M.1
Kwok, J.2
Kucera, S.3
Crook, R.4
Farrer, M.5
Houlden, H.6
Isaacs, A.7
Lincoln, S.8
Onstead, L.9
Hardy, J.10
Wittenberg, L.11
Dodd, P.12
Webb, S.13
Hayward, N.14
Tannenberg, T.15
Andreadis, A.16
Hallupp, M.17
Schofield, P.18
Dark, F.19
Hutton, M.20
more..
-
54
-
-
0030985991
-
A family with autosomal-dominant non-Alzheimer's presenile dementia
-
Dark F (1997) A family with autosomal-dominant non-Alzheimer's presenile dementia. Aust N Z J Psychiatry 31:706-715
-
(1997)
Aust N Z J Psychiatry
, vol.31
, pp. 706-715
-
-
Dark, F.1
-
55
-
-
19244362853
-
Linkage of frontotemporal dementia to chromosome 17: Clinical and neuropathological characterization of phenotype
-
Yamaoka LH, Welsh-Bohmer KA, Hulette CM, Gaskell PC, Murray M, Rimmler JL, Helms BR, Guerra M, Roses AD, Schmechel DE, Pericak-Vance MA (1996) Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype. Am J Hum Genet 59:1306-1312
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1306-1312
-
-
Yamaoka, L.H.1
Welsh-Bohmer, K.A.2
Hulette, C.M.3
Gaskell, P.C.4
Murray, M.5
Rimmler, J.L.6
Helms, B.R.7
Guerra, M.8
Roses, A.D.9
Schmechel, D.E.10
Pericak-Vance, M.A.11
-
56
-
-
0030887854
-
Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filaments
-
Spillantini MG, Goedert M, Crowther RA, Murrell JR, Farlow MJ, Ghetti B (1997) Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments. Proc Natl Acad Sci USA 94:4113-4118
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 4113-4118
-
-
Spillantini, M.G.1
Goedert, M.2
Crowther, R.A.3
Murrell, J.R.4
Farlow, M.J.5
Ghetti, B.6
-
57
-
-
0030826625
-
Autosomal-dominant dementia with widespread neurofibrillary tangles
-
Reed LA, Grabowski TJ, Schmidt ML, Morris L, Morris JC, Goate A, Solodkin A, Van Hoesen G, Schelper RL, Talbot CJ, Wragg MA, Trojanowski JQ (1997) Autosomal-dominant dementia with widespread neurofibrillary tangles. Ann Neurol 42:564-572
-
(1997)
Ann Neurol
, vol.42
, pp. 564-572
-
-
Reed, L.A.1
Grabowski, T.J.2
Schmidt, M.L.3
Morris, L.4
Morris, J.C.5
Goate, A.6
Solodkin, A.7
Van Hoesen, G.8
Schelper, R.L.9
Talbot, C.J.10
Wragg, M.A.11
Trojanowski, J.Q.12
-
59
-
-
0031738468
-
Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau
-
Spillantini MG, Crowther RA, Kamphorst W, Heutink P, Van Swieten JC (1998) Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau. Am J Pathol 153:1359-1363
-
(1998)
Am J Pathol
, vol.153
, pp. 1359-1363
-
-
Spillantini, M.G.1
Crowther, R.A.2
Kamphorst, W.3
Heutink, P.4
Van Swieten, J.C.5
-
60
-
-
0026595846
-
Tau proteins of Alzheimer paired helical filaments: Abnormal phosphorylation of all six brain isoforms
-
Goedert M, Spillantini MG, Cairns NJ, Crowther RA (1992) Tau proteins of Alzheimer paired helical filaments: abnormal phosphorylation of all six brain isoforms. Neuron 8:159-168
-
(1992)
Neuron
, vol.8
, pp. 159-168
-
-
Goedert, M.1
Spillantini, M.G.2
Cairns, N.J.3
Crowther, R.A.4
-
61
-
-
0030000867
-
Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles
-
Spillantini MG, Crowther RA, Goedert M (1996) Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles. Acta Neuropathol (Berl) 92:42-48
-
(1996)
Acta Neuropathol (Berl)
, vol.92
, pp. 42-48
-
-
Spillantini, M.G.1
Crowther, R.A.2
Goedert, M.3
-
62
-
-
0025676285
-
Presence of two different fibril subtypes in the Pick body: An immunoelectron microscopic study
-
Kato S, Nakamura H (1990) Presence of two different fibril subtypes in the Pick body: an immunoelectron microscopic study. Acta Neuropathol (Berl) 81:125-129
-
(1990)
Acta Neuropathol (Berl)
, vol.81
, pp. 125-129
-
-
Kato, S.1
Nakamura, H.2
-
64
-
-
0033055359
-
Stable expression in Chinese hamster ovary cells of mutated tau genes causing frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)
-
Matsumura N, Yamazaki T, Ihara Y (1999) Stable expression in Chinese hamster ovary cells of mutated tau genes causing frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Am J Pathol 154:1649-1656
-
(1999)
Am J Pathol
, vol.154
, pp. 1649-1656
-
-
Matsumura, N.1
Yamazaki, T.2
Ihara, Y.3
-
65
-
-
0027308924
-
Abnormal tau phosphorylation at ser396 in Alzheimer's disease recapitulates development and contributes to reduced microtubule binding
-
Bramblett GT, Goedert M, Jakes R, Merrick SE, Trojanowski JQ, Lee VM-Y (1993) Abnormal tau phosphorylation at Ser396 in Alzheimer's disease recapitulates development and contributes to reduced microtubule binding. Neuron 19:1089-1099
-
(1993)
Neuron
, vol.19
, pp. 1089-1099
-
-
Bramblett, G.T.1
Goedert, M.2
Jakes, R.3
Merrick, S.E.4
Trojanowski, J.Q.5
Lee, V.-Y.6
-
66
-
-
0027237861
-
Tau in paired helical filament is functionally distinct from fetal tau: Assembly incompetence of paired helical filament tau
-
Yoshida H, Ihara Y (1993) Tau in paired helical filament is functionally distinct from fetal tau: assembly incompetence of paired helical filament tau. J Neurochem 61:1183-1186
-
(1993)
J Neurochem
, vol.61
, pp. 1183-1186
-
-
Yoshida, H.1
Ihara, Y.2
-
67
-
-
0029907548
-
Assembly of microtubule-associated protein tau into Alzheimer-like filaments induced by sulphated glycosaminoglycans
-
Goedert M, Jakes R, Spillantini MG, Hasegawa M, Smith MJ, Crowther RA (1996) Assembly of microtubule-associated protein tau into Alzheimer-like filaments induced by sulphated glycosaminoglycans. Nature 383:550-553
-
(1996)
Nature
, vol.383
, pp. 550-553
-
-
Goedert, M.1
Jakes, R.2
Spillantini, M.G.3
Hasegawa, M.4
Smith, M.J.5
Crowther, R.A.6
-
68
-
-
0029796168
-
Polymerization of tau into filaments in the presence of heparin: The minimal sequence required for tautau interactions
-
Pérez M, Valpuesta JM, Medina M, Montejo de Garcini E, Avila J (1996) Polymerization of tau into filaments in the presence of heparin: the minimal sequence required for tautau interactions. J Neurochem 67:1183-1190
-
(1996)
J Neurochem
, vol.67
, pp. 1183-1190
-
-
Pérez, M.1
Valpuesta, J.M.2
Medina, M.3
Montejo De Garcini, E.4
Avila, J.5
-
69
-
-
0030590911
-
RNA stimulates aggregation of microtubule-associated protein tau into Alzheimer-like paired helical filaments
-
Kampers T, Friedhoff P, Biernat J, Mandelkow EM, Mandelkow E (1996) RNA stimulates aggregation of microtubule-associated protein tau into Alzheimer-like paired helical filaments. FEBS Lett 399:344-349
-
(1996)
FEBS Lett
, vol.399
, pp. 344-349
-
-
Kampers, T.1
Friedhoff, P.2
Biernat, J.3
Mandelkow, E.M.4
Mandelkow, E.5
-
70
-
-
0031439109
-
Alzheimer-like changes in microtubule-associated protein tau induced by sulfated glycosaminoglycans. Inhibition of microtubule binding, stimulation of phosphorylation, and filament assembly depend on the degree of sulfation
-
Hasegawa M, Crowther RA, Jakes R, Goedert M (1997) Alzheimer-like changes in microtubule-associated protein tau induced by sulfated glycosaminoglycans. Inhibition of microtubule binding, stimulation of phosphorylation, and filament assembly depend on the degree of sulfation. J Biol Chem 272:33118-33124
-
(1997)
J Biol Chem
, vol.272
, pp. 33118-33124
-
-
Hasegawa, M.1
Crowther, R.A.2
Jakes, R.3
Goedert, M.4
-
71
-
-
0032428153
-
A nucleated assembly mechanism of Alzheimer paired helical filaments
-
Friedhoff P, Bergen M von, Mandelkow EM, Davies P, Mandelkow E (1998) A nucleated assembly mechanism of Alzheimer paired helical filaments. Proc Natl Acad Sci U S A 95:15712-15717
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 15712-15717
-
-
Friedhoff, P.1
Von Bergen, M.2
Mandelkow, E.M.3
Davies, P.4
Mandelkow, E.5
-
72
-
-
0030923223
-
Free fatty acids stimulate the polymerization of tau and amyloid β peptides. In vitro evidence for a common effector of pathogenesis in Alzheimer's disease
-
Wilson DM, Binder LI (1997) Free fatty acids stimulate the polymerization of tau and amyloid β peptides. In vitro evidence for a common effector of pathogenesis in Alzheimer's disease. Am J Pathol 150:2181-2195
-
(1997)
Am J Pathol
, vol.150
, pp. 2181-2195
-
-
Wilson, D.M.1
Binder, L.I.2
-
73
-
-
0003986552
-
Isolation of a fragment of tau derived from the core of the paired helical filament of Alzheimer disease
-
Wischik CM, Novak M, Thogersen HC, Edwards PC, Runswick MJ, Jakes R, Walker JE, Milstein C, Roth M, Klug A (1988) Isolation of a fragment of tau derived from the core of the paired helical filament of Alzheimer disease. Proc Natl Acad Sci U S A 85:4506-4510
-
(1988)
Proc Natl Acad Sci U S A
, vol.85
, pp. 4506-4510
-
-
Wischik, C.M.1
Novak, M.2
Thogersen, H.C.3
Edwards, P.C.4
Runswick, M.J.5
Jakes, R.6
Walker, J.E.7
Milstein, C.8
Roth, M.9
Klug, A.10
-
74
-
-
0026017033
-
Structural aspects of pathology in Alzheimer's disease
-
Crowther RA (1991) Structural aspects of pathology in Alzheimer's disease. Biochim Biophys Acta 1069:1-9
-
(1991)
Biochim Biophys Acta
, vol.1069
, pp. 1-9
-
-
Crowther, R.A.1
-
75
-
-
0025863618
-
Neuropathological stageing of Alzheimer-related changes
-
Braak H, Braak E (1991) Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol (Berl) 82:239-259
-
(1991)
Acta Neuropathol (Berl)
, vol.82
, pp. 239-259
-
-
Braak, H.1
Braak, E.2
-
76
-
-
0030805991
-
Frequency of stages of Alzheimer-related lesions in different age categories
-
Braak H, Braak E (1997) Frequency of stages of Alzheimer-related lesions in different age categories. Neurobiol Aging 18:351-357
-
(1997)
Neurobiol Aging
, vol.18
, pp. 351-357
-
-
Braak, H.1
Braak, E.2
-
77
-
-
0025857173
-
Abnormal tau proteins in progressive supranuclear palsy. Similarities and differences with the neurofibrillary degeneration of the Alzheimer type
-
Flament S, Delacourte A, Vernay M, Hauw JJ, Javoy-Agid F (1991) Abnormal tau proteins in progressive supranuclear palsy. Similarities and differences with the neurofibrillary degeneration of the Alzheimer type. Acta Neuropathol (Berl) 81:591-596
-
(1991)
Acta Neuropathol (Berl)
, vol.81
, pp. 591-596
-
-
Flament, S.1
Delacourte, A.2
Vernay, M.3
Hauw, J.J.4
Javoy-Agid, F.5
-
78
-
-
0028091523
-
Ultra-structure and biochemical composition of paired helical filaments in corticobasal degeneration
-
Ksiezak-Reding H, Morgan K, Mattiace LA, Davies P, Liu W-K, Yen S-H, Weidenheim K, Dickson DW (1994) Ultra-structure and biochemical composition of paired helical filaments in corticobasal degeneration. Am J Pathol 145:1496-1508
-
(1994)
Am J Pathol
, vol.145
, pp. 1496-1508
-
-
Ksiezak-Reding, H.1
Morgan, K.2
Mattiace, L.A.3
Davies, P.4
Liu, W.-K.5
Yen, S.-H.6
Weidenheim, K.7
Dickson, D.W.8
-
79
-
-
0033009603
-
Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: Tau pathologies with exclusively "exon 10" isoforms
-
Sergeant N, Wattez, A, Delacourte A (1999) Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: Tau pathologies with exclusively "exon 10" isoforms. J Neurochem 72:1243-1249
-
(1999)
J Neurochem
, vol.72
, pp. 1243-1249
-
-
Sergeant, N.1
Wattez, A.2
Delacourte, A.3
-
80
-
-
0032859650
-
Overexpression of four-repeat tau mRNA isoforms in progressive supranuclear palsy but not in Alzheimer's disease
-
Chambers CB, Lee JM, Troncoso JC, Reich S, Muma NA (1999) Overexpression of four-repeat tau mRNA isoforms in progressive supranuclear palsy but not in Alzheimer's disease. Ann Neurol 46:325-332
-
(1999)
Ann Neurol
, vol.46
, pp. 325-332
-
-
Chambers, C.B.1
Lee, J.M.2
Troncoso, J.C.3
Reich, S.4
Muma, N.A.5
-
81
-
-
0031044850
-
Genetic evidence for the involvement of tau in progressive supranuclear palsy
-
Conrad C, Andreadis A, Trojanowski JQ, Dickson DW, Kang D, Chen X, Wiederholt W, Hansen L, Masliah E, Thal LJ, Katzman R, Xia Y, Saitoh T (1997) Genetic evidence for the involvement of tau in progressive supranuclear palsy. Ann Neurol 41:277-281
-
(1997)
Ann Neurol
, vol.41
, pp. 277-281
-
-
Conrad, C.1
Andreadis, A.2
Trojanowski, J.Q.3
Dickson, D.W.4
Kang, D.5
Chen, X.6
Wiederholt, W.7
Hansen, L.8
Masliah, E.9
Thal, L.J.10
Katzman, R.11
Xia, Y.12
Saitoh, T.13
-
82
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
Baker M, Litvan I, Houlden H, Adamson J, Dickson D, Perez-Tur J, Hardy J, Lynch T, Bigio E, Hutton M (1999) Association of an extended haplotype in the tau gene with progressive supranuclear palsy. Hum Mol Genet 8:711-715
-
(1999)
Hum Mol Genet
, vol.8
, pp. 711-715
-
-
Baker, M.1
Litvan, I.2
Houlden, H.3
Adamson, J.4
Dickson, D.5
Perez-Tur, J.6
Hardy, J.7
Lynch, T.8
Bigio, E.9
Hutton, M.10
-
83
-
-
0029670872
-
Specific pathological tau protein variants characterize Pick's disease
-
Delacourte A, Robitaille Y, Sergeant N, Buée L, Hof PR, Wattez A, Laroche-Cholette A, Mathieu J, Chagnon P, Gauvreau D (1996) Specific pathological tau protein variants characterize Pick's disease. J Neuropathol Exp Neurol 55:159-168
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 159-168
-
-
Delacourte, A.1
Robitaille, Y.2
Sergeant, N.3
Buée, L.4
Hof, P.R.5
Wattez, A.6
Laroche-Cholette, A.7
Mathieu, J.8
Chagnon, P.9
Gauvreau, D.10
-
84
-
-
0031935017
-
Vulnerable subsets in alzheimer's and Pick's disease are distinguished by their tau isoform distribution and phosphorylation
-
Delacourte A, Sergeant N, Wattez A, Gauvreau D, Robitaille Y (1998) Vulnerable subsets in Alzheimer's and Pick's disease are distinguished by their tau isoform distribution and phosphorylation. Ann Neurol 43:193-204
-
(1998)
Ann Neurol
, vol.43
, pp. 193-204
-
-
Delacourte, A.1
Sergeant, N.2
Wattez, A.3
Gauvreau, D.4
Robitaille, Y.5
-
85
-
-
0033549267
-
Tangled areas of Alzheimer brain have upregulated levels of exon 10 containing tau mRNA
-
Yasojima K, McGeer EG, McGeer PL (1999) Tangled areas of Alzheimer brain have upregulated levels of exon 10 containing tau mRNA. Brain Res 831:301-305
-
(1999)
Brain Res
, vol.831
, pp. 301-305
-
-
Yasojima, K.1
McGeer, E.G.2
McGeer, P.L.3
-
86
-
-
0032127543
-
Engineering protein kinases with distinct nucleotide specificities and inhibitor sensitivities by mutation of a single amino acid
-
Cohen P, Goedert M (1998) Engineering protein kinases with distinct nucleotide specificities and inhibitor sensitivities by mutation of a single amino acid. Chem Biol 5:R161-R164
-
(1998)
Chem Biol
, vol.5
-
-
Cohen, P.1
Goedert, M.2
-
87
-
-
0032821768
-
A GSK3-binding peptide from FRAT1 selectively inhibits the GSK3-catalysed phosphorylation of axin and β-catenin
-
Thomas GM, Frame S, Goedert M, Nathke I, Polakis P, Cohen P (1999) A GSK3-binding peptide from FRAT1 selectively inhibits the GSK3-catalysed phosphorylation of axin and β-catenin. FEBS Lett 458:247-251
-
(1999)
FEBS Lett
, vol.458
, pp. 247-251
-
-
Thomas, G.M.1
Frame, S.2
Goedert, M.3
Nathke, I.4
Polakis, P.5
Cohen, P.6
-
88
-
-
0033600242
-
The prolyl isomerase pin1 restores the function of Alzheimer-associated phosphorylated tau protein
-
Lu P-J, Wulf G, Zhou XZ, Davies P, Lu KP (1999) The prolyl isomerase Pin1 restores the function of Alzheimer-associated phosphorylated tau protein. Nature 399:784-788
-
(1999)
Nature
, vol.399
, pp. 784-788
-
-
Lu, P.-J.1
Wulf, G.2
Zhou, X.Z.3
Davies, P.4
Lu, K.P.5
-
90
-
-
0028965635
-
Somatodendritic localization and hyperphosphorylation of tau protein in transgenic mice expressing the longest human brain tau isoform
-
Götz J, Probst A, Spillantini MG, Schäfer T, Jakes R, Bürki K, Goedert M (1995) Somatodendritic localization and hyperphosphorylation of tau protein in transgenic mice expressing the longest human brain tau isoform. EMBO J 14:1304-1313
-
(1995)
EMBO J
, vol.14
, pp. 1304-1313
-
-
Götz, J.1
Probst, A.2
Spillantini, M.G.3
Schäfer, T.4
Jakes, R.5
Bürki, K.6
Goedert, M.7
-
91
-
-
0345580607
-
Transgenic expression of the shortest human tau affects its compartmentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease
-
Brion JP, Tremp G, Octave JN (1999) Transgenic expression of the shortest human tau affects its compartmentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease. Am J Pathol 154:255-270
-
(1999)
Am J Pathol
, vol.154
, pp. 255-270
-
-
Brion, J.P.1
Tremp, G.2
Octave, J.N.3
-
92
-
-
0033536163
-
Immunization with amyloid-ß attenuates Alzheimer-disease-like pathology in the PDAPP mouse
-
Schenk D, Barbour R, Dunn W, Gordon G, Grajeda H, Guido T, Hu K, Huang J, Johnson-Wood K, Khan K, Kholodenko D, Lee M, Liao Z, Lieberburg I, Motter R, Mutter L, Soriano F, Shopp G, Vasquez N, Vandevert C, Walker S, Wogulis M, Yednock T, Games D, Seubert P (1999) Immunization with amyloid-ß attenuates Alzheimer-disease-like pathology in the PDAPP mouse. Nature 400:173-177
-
(1999)
Nature
, vol.400
, pp. 173-177
-
-
Schenk, D.1
Barbour, R.2
Dunn, W.3
Gordon, G.4
Grajeda, H.5
Guido, T.6
Hu, K.7
Huang, J.8
Johnson-Wood, K.9
Khan, K.10
Kholodenko, D.11
Lee, M.12
Liao, Z.13
Lieberburg, I.14
Motter, R.15
Mutter, L.16
Soriano, F.17
Shopp, G.18
Vasquez, N.19
Vandevert, C.20
Walker, S.21
Wogulis, M.22
Yednock, T.23
Games, D.24
Seubert, P.25
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